A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6353786



Internal ID21011339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:187129877..187215201hg38UCSC Ensembl
chr2:187994604..188079928hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg3885325
hg1985325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18080743
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6353786
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer